KR101235497B1 - 신규 화합물 - Google Patents
신규 화합물 Download PDFInfo
- Publication number
- KR101235497B1 KR101235497B1 KR1020077021881A KR20077021881A KR101235497B1 KR 101235497 B1 KR101235497 B1 KR 101235497B1 KR 1020077021881 A KR1020077021881 A KR 1020077021881A KR 20077021881 A KR20077021881 A KR 20077021881A KR 101235497 B1 KR101235497 B1 KR 101235497B1
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- heteroaryl
- aryl
- cycloalkyl
- hydrogen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 0 C*C1=C(C)NC(*)=C(C(C)=O)C(NC)=[Mn]1 Chemical compound C*C1=C(C)NC(*)=C(C(C)=O)C(NC)=[Mn]1 0.000 description 21
- CNPGOONUQONHKI-ALCCZGGFSA-N CBc1nc(N(C(C=C2)=O)c(c(F)ccc3)c3F)c2c(C(C)C/C=C\C(C)=C)n1 Chemical compound CBc1nc(N(C(C=C2)=O)c(c(F)ccc3)c3F)c2c(C(C)C/C=C\C(C)=C)n1 CNPGOONUQONHKI-ALCCZGGFSA-N 0.000 description 1
- JWZHMQJLLRSVNF-CLFYSBASSA-N CC(/C=C\C(C1(C(C(C)=CC2)=CC2C(O)OC)N2C1)=C(N)N=C2[n]1c(CN)ccc1)=O Chemical compound CC(/C=C\C(C1(C(C(C)=CC2)=CC2C(O)OC)N2C1)=C(N)N=C2[n]1c(CN)ccc1)=O JWZHMQJLLRSVNF-CLFYSBASSA-N 0.000 description 1
- JMFBSQBNMSUETN-UHFFFAOYSA-N CC(CC1)CCN1C(CC1)CCN1c1nc(-c2cc(C(O)=O)ccc2C)c(C=CC(N2c(c(F)ccc3)c3F)=O)c2n1 Chemical compound CC(CC1)CCN1C(CC1)CCN1c1nc(-c2cc(C(O)=O)ccc2C)c(C=CC(N2c(c(F)ccc3)c3F)=O)c2n1 JMFBSQBNMSUETN-UHFFFAOYSA-N 0.000 description 1
- MVCUQTSFJJCIDJ-YRNVUSSQSA-N CCC(CC)Nc1nc(/C=C/CC)c(C=CC(N2c(c(F)ccc3)c3F)=O)c2n1 Chemical compound CCC(CC)Nc1nc(/C=C/CC)c(C=CC(N2c(c(F)ccc3)c3F)=O)c2n1 MVCUQTSFJJCIDJ-YRNVUSSQSA-N 0.000 description 1
- MNGMBGKHQRYLNJ-UHFFFAOYSA-N CCCCCc1ccc(C)c(-c2c(C=CC(N3c(c(F)ccc4)c4F)=O)c3nc(N(CC3)CCC3C3CCC(C)CC3)n2)c1 Chemical compound CCCCCc1ccc(C)c(-c2c(C=CC(N3c(c(F)ccc4)c4F)=O)c3nc(N(CC3)CCC3C3CCC(C)CC3)n2)c1 MNGMBGKHQRYLNJ-UHFFFAOYSA-N 0.000 description 1
- HJJOSJPGSQFZKI-UHFFFAOYSA-N CCCCNC(NC)NCCC(C)(CCO)C=C Chemical compound CCCCNC(NC)NCCC(C)(CCO)C=C HJJOSJPGSQFZKI-UHFFFAOYSA-N 0.000 description 1
- KKTBUCVHSCATGB-UHFFFAOYSA-N CNC1CCCC1 Chemical compound CNC1CCCC1 KKTBUCVHSCATGB-UHFFFAOYSA-N 0.000 description 1
- XTSVTLOWTXKOLD-UHFFFAOYSA-N Cc(c(-c1c(C=CC(N2c(c(F)ccc3)c3F)=O)c2nc(NCc2ncc[nH]2)n1)c1)ccc1C(NC1CC1)=O Chemical compound Cc(c(-c1c(C=CC(N2c(c(F)ccc3)c3F)=O)c2nc(NCc2ncc[nH]2)n1)c1)ccc1C(NC1CC1)=O XTSVTLOWTXKOLD-UHFFFAOYSA-N 0.000 description 1
- DYWSZXDQVJZGBA-UHFFFAOYSA-N Cc(ccc(C(O)=O)c1)c1-c1c(C=CC(N2c(c(F)ccc3)c3F)=O)c2nc(SC)n1 Chemical compound Cc(ccc(C(O)=O)c1)c1-c1c(C=CC(N2c(c(F)ccc3)c3F)=O)c2nc(SC)n1 DYWSZXDQVJZGBA-UHFFFAOYSA-N 0.000 description 1
- FFXSYKVMQNWPCD-UHFFFAOYSA-N Cc1cc(C(Nc(cc2-c3c(C=CC(N4c(c(F)ccc5)c5F)=O)c4nc(SC)n3)ccc2C#N)=O)ccc1F Chemical compound Cc1cc(C(Nc(cc2-c3c(C=CC(N4c(c(F)ccc5)c5F)=O)c4nc(SC)n3)ccc2C#N)=O)ccc1F FFXSYKVMQNWPCD-UHFFFAOYSA-N 0.000 description 1
- JXDCMNODVYNKQS-UHFFFAOYSA-N ICCNC1CC1 Chemical compound ICCNC1CC1 JXDCMNODVYNKQS-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Cardiology (AREA)
- Pulmonology (AREA)
- Neurology (AREA)
- Heart & Thoracic Surgery (AREA)
- Oncology (AREA)
- Dermatology (AREA)
- Hematology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Communicable Diseases (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Obesity (AREA)
- Vascular Medicine (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Ophthalmology & Optometry (AREA)
- Transplantation (AREA)
- Toxicology (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US66531505P | 2005-03-25 | 2005-03-25 | |
US60/665,315 | 2005-03-25 | ||
PCT/US2006/010855 WO2006104915A2 (en) | 2005-03-25 | 2006-03-24 | 8-PHENYL-7,8-DIHYDROPYRIDO[2,3-d]PYRIMIDIN-7-ONES AND THEIR USE AS PHARMACEUTICALS |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20070113255A KR20070113255A (ko) | 2007-11-28 |
KR101235497B1 true KR101235497B1 (ko) | 2013-02-20 |
Family
ID=37053943
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020077021881A Expired - Fee Related KR101235497B1 (ko) | 2005-03-25 | 2006-03-24 | 신규 화합물 |
Country Status (24)
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7235551B2 (en) * | 2000-03-02 | 2007-06-26 | Smithkline Beecham Corporation | 1,5-disubstituted-3,4-dihydro-1h-pyrimido[4,5-d]pyrimidin-2-one compounds and their use in treating csbp/p38 kinase mediated diseases |
DK1333833T3 (da) * | 2000-10-23 | 2011-12-12 | Glaxosmithkline Llc | Ny trisubstitueret 8H-pyridol[2,3-d]pyrimidin-7-on-forbindelse til behandling af CSBP/RK/p38-kinnasemedierede sygdomme |
AU2003225072A1 (en) * | 2002-04-19 | 2003-11-03 | Smithkline Beecham Corporation | Novel compounds |
TWI389690B (zh) | 2005-03-25 | 2013-03-21 | Glaxo Group Ltd | 新穎化合物(一) |
WO2006110298A2 (en) * | 2005-03-25 | 2006-10-19 | Glaxo Group Limited | 8-alkyl/aryl-4-aryl-2-n- (alkylamino)-n'-substituted-n'-cyanoguanidino-8h-pyrido[2,3-d]pyrimidin-7-one compounds and use thereof |
PE20061193A1 (es) * | 2005-03-25 | 2006-12-02 | Glaxo Group Ltd | DERIVADOS DE 3,4-DIHIDROPIRIMIDO[4,5-d]PIRIMIDIN-2-[1H]-0NA COMO INHIBIDORES DE QUINASA p38 |
CA2603163A1 (en) * | 2005-03-25 | 2006-10-05 | Glaxo Group Limited | Process for preparing pyrido[2,3-d]pyrimidin-7-one and 3,4-dihydropyrimido[4,5-d]pyrimidin-2(1h)-one derivatives |
EP2034838A4 (en) * | 2006-06-16 | 2012-01-04 | Glaxo Group Ltd | NOVEL CONNECTIONS |
EP2032142A4 (en) * | 2006-06-16 | 2010-07-21 | Glaxo Group Ltd | NOVEL CONNECTIONS |
GB0621830D0 (en) * | 2006-11-02 | 2006-12-13 | Chroma Therapeutics Ltd | Inhibitors of p38 mitogen-activated protein kinase |
EP1992344A1 (en) | 2007-05-18 | 2008-11-19 | Institut Curie | P38 alpha as a therapeutic target in pathologies linked to FGFR3 mutation |
WO2012158197A2 (en) * | 2010-11-11 | 2012-11-22 | Lyndor Biosciences L.L.C. | Compounds useful as akt/pkb modulators and uses thereof |
EP2748147B1 (en) * | 2011-08-25 | 2017-08-02 | St. Jude Children's Research Hospital | Substituted 2-alkyl-1-oxo-n-phenyl-3-heteroaryl-1,2,3,4-tetrahydroisoquinoline-4-carboxamides for antimalarial therapies |
US10342786B2 (en) | 2017-10-05 | 2019-07-09 | Fulcrum Therapeutics, Inc. | P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD |
SG11202003035SA (en) | 2017-10-05 | 2020-04-29 | Fulcrum Therapeutics Inc | Use of p38 inhibitors to reduce expression of dux4 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030092712A1 (en) | 2000-12-20 | 2003-05-15 | Doherty James B. | (Halo-benzo carbonyl)heterocyclo fused phenyl p38 kinase inhibiting agents |
JP2004517922A (ja) | 2000-10-23 | 2004-06-17 | スミスクライン・ビーチャム・コーポレイション | 新規化合物 |
Family Cites Families (206)
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US25386A (en) | 1859-09-13 | Fastening fob | ||
US2833779A (en) | 1956-10-29 | 1958-05-06 | American Cyanamid Co | Substituted pyrazoles |
US2918408A (en) | 1957-04-08 | 1959-12-22 | Lakeside Lab Inc | Anti-spasmodic compositions specific for treating spasm of the colon |
US3631045A (en) | 1969-11-04 | 1971-12-28 | American Home Prod | 4 5-diamino-7h-pyrrolo(2 3-d)pyrimidine derivatives |
US3910913A (en) | 1969-11-04 | 1975-10-07 | American Home Prod | 4,5-Diamino-7H-pyrrolo{8 2,3-d{9 pyrimidine derivatives |
US3707475A (en) | 1970-11-16 | 1972-12-26 | Pfizer | Antiinflammatory imidazoles |
US3929807A (en) | 1971-05-10 | 1975-12-30 | Ciba Geigy Corp | 2-Substituted-4(5)-(aryl)-5(4)-(2,3 or -4-pyridyl)-imidazoles |
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